EP0687291B2

EP0687291B2 - Concentrated biodegradable quaternary ammonium fabric softener compositions and compounds containing intermediate iodine value unsaturated fatty acid chains

Info

Publication number: EP0687291B2
Application number: EP94910160A
Authority: EP
Inventors: Errol Hoffman Wahl; Dennis Ray Bacon; Ellen Schmidt Baker; Jean-François Bodet; Michael Eugene Burns; Hugo Jean Marie Demeyere; Charles Albert Hensley; Robert Mermelstein; John Cort Severns; John Henry Shaw, Jr.; Michael Peter Siklosi; Alice Marie Vogel; Jeffrey Wayne Watson
Original assignee: Procter and Gamble Co
Current assignee: Procter and Gamble Co
Priority date: 1993-03-01
Filing date: 1994-02-23
Publication date: 2005-08-24
Anticipated expiration: 2014-02-23
Also published as: NO953415D0; AU6271294A; DE69423963T2; ATE191743T1; CN1288985A; US5562849A; EP0687291A1; JPH08507766A; JP2006138063A; CA2157178C; DK0687291T4; FI954084A; CA2157178A1; ES2144515T5; DE69423963D1; PT687291E; GR3033212T3; US5545340A; FI954084A0; NO305020B1

Abstract

The present invention relates to softening compounds; stable, homogeneous, preferably concentrated, aqueous liquid and solid textile treatment compositions; and intermediate compositions and/or processes for making said compositions. The compositions of the present invention contain diester quaternary ammonium compounds wherein the fatty acyl groups have an Iodine Value of from greater than about 5 to less than about 100, a cis/trans isomer weight ratio of greater than about 30/70 when the Iodine Value is less than about 25, the level of unsaturation being less than about 65% by weight, wherein said compounds are capable of forming concentrated aqueous compositions with concentrations greater than about 13% by weight at an Iodine Value of greater than about 10 without viscosity modifiers other than normal polar organic solvents present in the raw material of the compound or added electrolyte.

Description

CROSS-REFERENCE TO RELATED APPLICATION

This is a continuation-in-part of our U.S. Patent Application Ser. No. 08/024,541, filed March 1, 1993, having the same title.

TECHNICAL FIELD

The present invention relates to softening compounds; stable, homogeneous, preferably concentrated, aqueous liquid and solid textile treatment compositions; and intermediate compositions and/or processes for making said compositions. In particular, it especially relates to textile softening compounds and compositions for use in the rinse cycle of a textile laundering operation to provide excellent fabric softening/static control benefits, the compositions being characterized by excellent storage and viscosity stability, as well as biodegradability.

BACKGROUND OF THE INVENTION

The art discloses many problems associated with formulating and preparing stable fabric conditioning formulations. See, for example, U.S. Pat. No. 3,904,533, Neiditch et al. issued Sept. 9, 1975. Japanese Laid Open Publication 1,249,129, filed Oct. 4, 1989, discloses a problem with dispersing fabric softener actives containing two long hydrophobic chains interrupted by ester linkages ("diester quaternary ammonium compounds") and solves it by rapid mixing. U.S. Pat. No. 5,066,414, Chang, issued Nov. 19, 1991, teaches and claims compositions containing mixtures of quaternary ammonium salts containing at least one ester linkage, nonionic surfactant such as a linear alkoxylated alcohol, and liquid carrier for improved stability and dispersibility. U.S. Pat. No. 4,767,547, Straathof et al., issued Aug. 30, 1988, claims compositions containing either diester, or monoester quaternary ammonium compounds where the nitrogen has either one, two, or three methyl groups, stabilized by maintaining a critical low pH of from 2.5 to 4.2.
U.S. Pat. No. 4,401,578, Verbruggen, issued Aug. 30, 1983 discloses hydrocarbons, fatty acids, fatty acid esters, and fatty alcohols as viscosity control agents for fabric softeners (the fabric softeners are disclosed as optionally comprising ester linkages in the hydrophobic chains). WO 89/115 22-A (DE 3.818,061-A; EP-346,634-A), with a priority of May 27, 1988, discloses diester quaternary ammonium fabric softener components plus a fatty acid. European Pat. No. 243,735 discloses sorbitan esters plus diester quaternary ammonium compounds to improve dispersions of concentrated softener compositions.
Diester quaternary ammonium compounds with a fatty acid, alkyl sulfate, or alkyl sulfonate anion are disclosed in European Pat. No. 336,267-A with a priority of April 2, 1988. U.S. Pat. No. 4,808,321, Walley, issued Feb. 28, 1989, teaches fabric softener compositions comprising monoester analogs of ditallow dimethyl ammonium chloride which are dispersed in a liquid carrier as sub-micron particles through high shear mixing, or particles can optionally be stabilized with emulsifiers such as nonionic C_14-18 ethoxylates.
E.P. Appln. 243,735, Nusslein et al., published Nov. 4, 1987, discloses sorbitan ester plus diester quaternary ammonium compounds to improve dispersibility of concentrated dispersions.
E.P. Appln. 409,502, Tandela et al., published Jan. 23, 1991, discloses, e.g., ester quaternary ammonium compounds, and a fatty acid material or its salt.
E.P. Appln. 240,727, Nusslein et al., priority date of March 12, 1986, teaches diester quaternary ammonium compounds with soaps or fatty acids for improved dispersibility in water.
The art also teaches compounds that alter the structure of diester quaternary ammonium compounds by substituting, e.g., a hydroxy ethyl for a methyl group or a polyalkoxy group for the alkoxy group in the two hydrophobic chains. Specifically, U.S. Pat. No. 3,915,867, Kang et al., issued Oct. 28, 1975, discloses the substitution of a hydroxyethyl group for a methyl group. A softener material with specific cis/trans content in the long hydrophobic groups is disclosed in Jap. Pat. Appln. 63-194316, filed Nov. 21, 1988. Jap. Pat. Appln. 4-333,667, published Nov. 20, 1992, teaches liquid softener compositions containing diester quaternary ammonium compounds having a total saturated:unsaturated ratio in the ester alkyl groups of 2:98 to 30:70.
All of the above patents and patent applications are incorporated herein by reference.

SUMMARY OF THE INVENTION

The present invention provides biodegradable textile softening compositions and compounds with excellent concentratability, static control, softening, and storage stability of concentrated aqueous compositions. In addition, these compositions provide these benefits under worldwide laundering conditions and minimize the use of extraneous ingredients for stability and static control to decrease environmental chemical load.
The compounds of the present invention, as defined in Claim 1 and 2, are quaternary ammonium compounds wherein the fatty acyl groups have an IV of from greater than 5 to less than 100, a cis/trans isomer weight ratio of greater than 30/70 when the IV is less than 25, the level of unsaturation being less than 65% by weight, wherein said compounds are capable of forming concentrated aqueous compositions with concentrations greater than 13% by weight at an IV of greater than 10 without viscosity modifiers other than normal polar organic solvents present in the raw material of the compound or added electrolyte, and wherein any fatty acyl groups from tallow must be modified.
The compositions can be aqueous liquids, preferably concentrated, containing from 5% to 50%, preferably from 15% to 40%, more preferably from 15% to 35%, and even more preferably from 15% to 32%, of said biodegradable, preferably diester, softening compound, or can be further concentrated to particulate solids, containing from 50% to 95%, preferably from 60% to 90%, of said softening compound.
Water can be added to the particulate solid compositions to form dilute or concentrated liquid softener compositions with a concentration of said softening compound of from 5% to 50%, preferably from 5% to 35%, more preferably from 5% to 32%. The particulate solid composition can also be used directly in the rinse bath to provide adequate usage concentration (e.g., from 10 to 1,000 ppm, preferably from 50 to 500 ppm, of total active ingredient). The liquid compositions can be added to the rinse to provide the same usage concentrations. Providing the composition in solid form provides cost savings on shipping the product (less weight) and cost savings on processing the composition (less shear and heat input needed to process the solid form).
The present invention also provides a process for preparation of concentrated aqueous biodegradable textile softener compositions (dispersions) with excellent de-watering of the softener vesicles in said dispersions, involving a two-stage addition of electrolyte which results in more water in the continuous phase and greater fluidity of said concentrated aqueous compositions. This process also involves the addition of perfume at lower than conventional temperatures which retards partitioning of certain perfume components into the softener vesicles, and thereby promotes viscosity stability. In addition, adding perfume to concentrated liquid fabric softeners, at ambient temperature, in a separate mixing vessel minimizes their volatilization and cross-contamination between batches and simplifies the manufacturing operation.

DETAILED DESCRIPTION OF THE INVENTION

(A) Diester Quaternary Ammonium Compound (DEQA)

The present invention relates to DEQA compounds and compositions containing DEQA as an essential component: DEQA having the formula: (R)_4-m - N⁺ - [(CH₂)_n - Y - R²]_m X^- wherein
each Y = -O-(O)C-, or -C(O)-O-;
m = 2;
each n = 1 to 4;
each R substituent is a short chain C₁-C₆, preferably C₁-C₃, alkyl group, e.g., methyl (most preferred), ethyl, propyl, and the like, benzyl or mixtures thereof;
each R² is a long chain, at least partially unsaturated (IV of greater than 5 to less than 100), C₁₁-C₂₁ hydrocarbyl, or substituted hydrocarbyl substituent and the counterion, X^-, can be any softener-compatible anion, for example, chloride, bromide, methylsulfate, formate, sulfate, nitrate and the like.
DEQA compounds prepared with fully saturated acyl groups are rapidly biodegradable and excellent softeners. However, it has now been discovered that compounds prepared with at least partially unsaturated acyl groups have many advantages (i.e., concentratability and good storage viscosity) and are highly acceptable for consumer products when certain conditions are met.
Variables that must be adjusted to obtain the benefits of using unsaturated acyl groups include the lodine Value (IV) of the fatty acids; the cis/trans isomer weight ratios in the fatty acyl groups; and the odor of fatty acid and/or the DEQA. Any reference to IV values hereinafter refers to IV (Iodine Value) of fatty acyl groups and not to the resulting DEQA compound.
When the IV of the fatty acyl groups is above 20, the DEQA provides excellent antistatic effect. Antistatic effects are especially important where the fabrics are dried in a tumble dryer, and/or where synthetic materials which generate static are used. Maximum static control occurs with an IV of greater than 20, preferably greater than 40. When fully saturated DEQA compositions are used, poor static control results. Also, as discussed hereinafter, concentratability increases as IV increases. The benefits of concentratability include: use of less packaging material; use of less organic solvents, especially volatile organic solvents; use of less concentration aids which may add nothing to performance; etc.
As the IV is raised, there is a potential for odor problems. Surprisingly, some highly desirable, readily available sources of fatty acids such as tallow, possess odors that remain with the compound DEQA despite the chemical and mechanical processing steps which convert the raw tallow to finished DEOA. Such sources must be deodorized, e.g., by absorption, distillation (including stripping such as steam stripping), etc., as is well known in the art. In addition, care must be taken to minimize contact of the resulting fatty acyl groups to oxygen and/or bacteria by adding antioxidants, antibacterial agents, etc. The additional expense and effort associated with the unsaturated fatty acyl groups is justified by the superior concentratability and/or performance which was not heretofore recognized. For example, DEQA containing unsaturated fatty acyl groups can be concentrated above about 13% without the need for additional concentration aids, especially surfactant concentration aids as discussed hereinafter.
DEQA derived from highly unsaturated fatty acyl groups, i.e., fatty acyl groups having a total unsaturation above 65% by weight, do not provide any additional improvement in antistatic effectiveness. They may, however, able to provide other benefits such as improved water absorbency of the fabrics. In general, an IV range of from 40 to 65 is preferred for concentratability, maximization of fatty acyl sources, excellent softness, static control, etc.
Highly concentrated aqueous dispersions of these diester compounds can gel and/or thicken during low 4.44°C (40°F) temperature storage. Diester compounds made from only unsaturated fatty acids minimizes this problem but additionally is more likely to cause malodor formation. Surprisingly, compositions from these diester compounds made from fatty acids having an IV of from 5 to 25, preferably from 10 to 25, more preferably from 15 to 20, and a cis/trans isomer weight ratio of from 70/30 or greater are storage stable at low temperature with minimal odor formation. These cis/trans isomer weight ratios provide optimal concentratability at these IV ranges. In the IV range above 25, the ratio of cis to trans isomers is less important unless higher concentrations are needed. The relationship between IV and concentratability is described hereinafter. For any IV, the concentration that will be stable in an aqueous composition will depend on the criteria for stability (e.g., stable down to 5°C; stable down to 0°C; doesn't gel; gels but recovers on heating, etc.) and the other ingredients present, but the concentration that is stable can be raised by adding the concentration aids, described hereinafter in more detail, to achieve the desired stability.
Generally, hydrogenation of fatty acids to reduce polyunsaturation and to lower IV to insure good color and improve odor and odor stability leads to a high degree of trans configuration in the molecule. Therefore, diester compounds derived from fatty acyl groups having low IV values can be made by mixing fully hydrogenated fatty acid with touch hydrogenated fatty acid at a ratio which provides an IV of from 5 to 25. The polyunsaturation content of the touch hardened fatty acid should be less than 5%, preferably less than 1%. During touch hardening the cis/trans isomer weight ratios are controlled by methods known in the art such as by optimal mixing, using specific catalysts, providing high H₂ availability, etc. Touch hardened fatty acid with high cis/trans isomer weight ratios is available commercially (i.e., Radiacid 406 from FINA).
It has also been found that for good chemical stability of the diester quaternary compound in molten storage, moisture level in the raw material must be controlled and minimized preferably less than 1 % and more preferably less than 0.5% water. Storage temperatures should be kept low as possible and still maintain a fluid material, ideally in the range of from 48.9°C (120F) to 65.6°C (150°F). The optimum storage temperature for stability and fluidity depends on the specific IV of the fatty acid used to make the diester quaternary and the level/type of solvent selected. It is important to provide good molten storage stability to provide a commercially feasible raw material that will not degrade noticeably in the normal transportation/storage/handling of the material in manufacturing operations.
Compositions of the present invention contain the following levels of DEQA:
I. for solid compositions: from 50% to 95%, preferably from 60% to 90%, and
II. for liquid compositions: from 5% to 50%, preferably from 15% to 40%, more preferably from 15% to 35%, and even more preferably from 15% to 32%.
It will be understood that substituent R² can optionally be substituted with various groups such as alkoxyl or hydroxyl groups. The preferred compounds can be considered to be diester variations of ditallow dimethyl ammonium chloride (DTDMAC), which is a widely used fabric softener. At least 80% of the DEQA is in the diester form, and from 0% to 20%, preferably less than 10%, more preferably less than 5%, can be DEQA monoester (e.g., only one -Y-R² group).
As used herein, when the diester is specified, it will include the monoester that is normally present. For softening, under no/low detergent carry-over laundry conditions the percentage of monoester should be as low as possible, preferably no more than 2.5%. However, under high detergent carry-over conditions, some monoester is preferred. The overall ratios of diester to monoester are from 100:1 to 2:1, preferably from 50:1 to 5:1, more preferably from 13:1 to 8:1. Under high detergent carry-over conditions, the di/monoester ratio is preferably 11:1. The level of monoester present can be controlled in the manufacturing of the DEQA.
DEQA compounds prepared with saturated acyl groups, i.e., having an IV of 5 or less, can be partially substituted for the DEQA compounds of the present invention prepared with unsaturated acyl groups having an IV of greater than 20. This partial substitution can decrease the odor associated with unsaturated DEQA. The ratio is from 0.2:1 to about 8:1, preferably from 0,25:1 to 4:1, most preferably from 0.3:1 to 1.5:1.
The following are non-limiting examples (wherein all long-chain alkyl substituents are straight-chain):

Saturated

[C₂H₅]₂N [CH₂CH₂OC(O)C₁₇H₃₅]₂ Cl^- [CH₃] [C₂H₅]⁺N[CH₂CH₂OC(O)C₁₃H₂₇]₂ I^- [C₃H₇] [C₂H₅]⁺N[CH₂CH₂OC(O)C₁₅H₃₁]₂ SO₄CH₃
[CH₃]₂ ⁺N[CH₂CH₂OC(O)R²]₂ Cl^- where -C(O)R² is derived from saturated tallow.

Unsaturated

[C₂H₅]₂ ⁺N [CH₂CH₂OC(O)C₁₇H₃₃]₂ Cl^- [CH₃] [C₂H₅]⁺N[CH₂CH₂OC(O)C₁₃H₂₅]₂ I^- [C₃H₇] [C₂H₅]⁺N[CH₂CH₂OC(O)C₁₅H₂₄]₂ SO₄ ^-CH₃
[CH₃]₂ ⁺N[CH₂CH₂OC(O)R²]₂ Cl^- where -C(O)R² is derived from partially hydrogenated tallow having the characteristics set forth herein.
It is especially surprising that careful pH control can noticeably improve product odor stability of compositions using unsaturated DEQA.
In addition, since the foregoing compounds (diesters) are somewhat labile to hydrolysis, they should be handled rather carefully when used to formulate the compositions herein. For example, stable liquid compositions herein are formulated at a pH in the range of from 2 to 5, preferably from 2 to 4.5, more preferably from 2 to 4. For best product odor stability, when the IV is greater that 25, the pH is from 2.8 to 3.5, especially for "unscented" (no perfume) or lightly scented products. This appears to be true for all DEQAs, but is especially true tor the preferred DEQA specified herein, i.e., having an IV of greater than 20, preferably greater than 40. The limitation is more important as IV increases. The pH can be adjusted by the addition of a Bronsted acid. The pH ranges above are determined without prior dilution of the composition with water.
Examples of suitable Bronsted acids include the inorganic mineral acids, carboxylic acids, in particular the low molecular weight (C₁-C₅) carboxylic acids, and alkylsulfonic acids. Suitable inorganic acids include HCl, H₂SO₄, HNO₃ and H₃PO₄. Suitable organic acids include formic, acetic, methylsulfonic and ethylsulfonic acid. Preferred acids are hydrochloric, phosphoric, and citric acids.

Synthesis of a Diester Quaternary Ammonium Compound

Synthesis of a preferred biodegradable, diester quaternary, ammonium softening compound used herein can be accomplished by the following two-step process:

Step A. Synthesis of Amine

RC(O) = Derived from Deodorized Soft Tallow (touch hardened)

Amine

N-Methyldiethanolamine (440.9 g, 3.69 mol) and triethylamine (561.2 g, 5.54 mol) are dissolved in CH₂Cl₂ (12 L) in a 22 L 3-necked flask equipped with an addition funnel, thermometer, mechanical stirrer, condenser, and an argon sweep. Deodorized, touch hardened, soft tallow fatty acid chloride (2.13 kg, 7.39 mol) is dissolved in 2 L CH₂Cl₂ and added slowly to the amine solution. The amine solution is then heated to 35°C to keep the talloyl chloride in solution as it is added. The addition of the acid chloride increased the reaction temperature to reflux (40°C). The acid chloride addition is slow enough to maintain reflux but not so fast as to lose methylene chloride out of the top of the condenser. The addition should take place over 1.5 hours. The solution is heated at reflux an additional 3 hours. The heat is removed and the reaction stirred 2 hours to cool to room temperature. CHCl₃ (12 L) is added. This solution is washed with 1 gallon of saturated NaCl and 1 gallon of saturated Ca(OH)₂. The organic layer is allowed to set overnight at room temperature. It is then extracted three times with 50% K₂CO₃ (7.6 L (2 gal). each). This is followed by 2 saturated NaCl washes (7.6 L (2 gal). each). Any emulsion that formed during these extractions is resolved by addition of CHCl₃ and/or saturated salt and heating on a steam bath. The organic layer is then dried with MgSO₄, filtered and concentrated down. Yield is 2.266 kg of soft tallow precursor amine diester. TLC silica (75% Et₂O/25% hexane one spot at Rf 0.69).

Step B. Quaternization

Soft tallow precursor amine (2.166 kg, 3.47 mol) is heated on a steam bath with CH₃CN 3.8 L (1 gal.) until it becomes fluid. The mixture is then poured into a 38L (10 gal.), glass-lined, stirred Pfaudler reactor containing CH₃CN (15.12L) (4 gal.). CH₃Cl (25 lbs., liquid) was added via a tube and the reaction is heated to 80°C for 6 hours. The CH₃CN/amine solution is removed from the reactor, filtered and the solid allowed to dry at room temperature over the weekend. The filtrate is roto-evaporated down, allowed to air dry overnight and combined with the other solid. Yield: 2.125 kg white powder.
Diester quaternary ammonium softening compounds can also be synthesized by other processes:
0.6 mole of diethanol methyl amine is placed in a 3-liter, 3-necked flask equipped with a reflux condenser, argon (or nitrogen) inlet and two addition funnels. In one addition funnel is placed 0.4 moles of triethylamine and in the second addition funnel is placed 1.2 moles of palmitoyl chloride in a 1:1 solution with methylene chloride. Methylene chloride (750 mL) is added to the reaction flask containing the amine and heated to 35°C (water bath). The triethylamine is added dropwise, and the temperature is raised to 40°-45°C while stirring over one-half hour. The palmitoyl chloride/methylene chloride solution is added dropwise and allowed to heat at 40°-45°C under inert atmosphere overnight (12-16 h).
The reaction mixture is cooled to room temperature and diluted with chloroform (1500 ml). The chloroform solution of product is placed in a separatory funnel (4 L) and washed with saturated NaCl, diluted Ca(OH)₂, 50% K₂CO₃ (3 times)*, and, finally, saturated NaCl. The organic layer is collected and dried over MgSO₄, filtered and solvents are removed via rotary evaporation. Final drying is done under high vacuum (0.25 mm Hg).

Step B. Quaternization

0.5 moles of the methyl diethanol palmitoleate amine from Step A is placed in an autoclave sleeve along with 200-300 mL of acetonitrile (anhydrous). The sample is then inserted into the autoclave and purged three times with N₂ (16275 mm Hg/21.4 ATM) and once with CH₃Cl. The reaction is heated to 80°C under a pressure of 3604 mm Hg/4.7 ATM in CH₃Cl for 24 hours. The autoclave sleeve is then removed from the reaction mixture. The sample is dissolved in chloroform and solvent is removed by rotary evaporation, followed by drying on high vacuum (0.25 mm Hg).
Another process by which the preferred diester quaternary compound can be made commercially is the reaction of fatty acids (e.g., tallow fatty acids) with methyl diethanolamine. Well known reaction methods are used to form the amine diester precursor. The diester quaternary is then formed by reaction with methyl chloride as previously discussed.
The above reaction processes are generally known in the art for the production of diester softening compounds. To achieve the IV, cis/trans ratios, and percentage unsaturation outlined above, usually additional modifications to these processes must be made.

(B) Optional Viscosity/Dispersibility Modifiers

As stated before, relatively concentrated compositions of the unsaturated DEQA can be prepared that are stable without the addition of concentration aids. However, the compositions of the present invention require organic and/or inorganic concentration aids to go to even higher concentrations and/or to meet higher stability standards depending on the other ingredients. These concentration aids which typically can be viscosity modifiers may be needed, or preferred, for ensuring stability under extreme conditions when particular softener active levels in relation to IV are present.
This relationship between IV and the concentration where concentration aids are needed in a typical aqueous liquid fabric softener composition containing perfume can be defined, at least approximately, by the following equation (for IVs of from greater than 25 to less than 100): Concentration of Softener Active (Wt%) = 4.85 + 0.838 (IV) - 0.00756 (IV)² (where R² = 0.99). Above these softener active levels, concentration aids are needed. These numbers are only approximations and if other variables of the formulation change, such as solvent, other ingredients, fatty acids, etc., concentration aids may be required for slightly lower concentrations or not required for slightly higher concentrations. For non-perfume or low level perfume compositions ("unscented" compositions), higher concentrations are possible at given IV levels. If the formulation separates, concentration aids can be added to achieve the desired criteria.

I. Surfactant Concentration Aids

The surfactant concentration aids are typically selected from the group consisting of (1) single long chain alkyl cationic surfactants; (2) nonionic surfactants; (3) amine oxides; (4) fatty acids; or (5) mixtures thereof. The levels of these aids are described below.

(1) The Single-Long-Chain Alkyl Cationic Surfactant

The mono-long-chain-alkyl (water-soluble) cationic surfactants:
I. in solid compositions are at a level of from 0% to 15%, preferably from 3% to 15%, more preferably from 5% to 15%, and
II. in liquid compositions are at a level of from 0% to 15%, preferably from 0.5% to 10%, the total single-long-chain cationic surfactant being at least at an effective level.
Such mono-long-chain-alkyl cationic surfactants useful in the present invention are, preferably, quaternary ammonium salts of the general formula: [R²N⁺R₃]X^- wherein the R² group is C₁₀-C₂₂ hydrocarbon group, preferably C₁₂-C₁₈ alkyl group or the corresponding ester linkage interrupted group with a short alkylene (C₁-C₄) group between the ester linkage and the N, and having a similar hydrocarbon group, e.g., a fatty acid ester of choline, preferably C₁₂-C₁₄ (coco) choline ester and/or C₁₆-C₁₈ tallow choline ester at from 0.1% to 20% by weight of the softener active. Each R is a C₁-C₄ alkyl or substituted (e.g., hydroxy) alkyl, or hydrogen, preferably methyl, and the counterion X^- is a softener compatible anion, for example, chloride, bromide, methyl sulfate, etc.
The ranges above represent the amount of the single-long-chain-alkyl cationic surfactant which is added to the composition of the present invention. The ranges do not include the amount of monoester which is already present in component (A), the diester quaternary ammonium compound, the total present being at least at an effective level.
The long chain group R², of the single-long-chain-alkyl cationic surfactant, typically contains an alkylene group having from 10 to 22 carbon atoms, preferably from 12 to 16 carbon atoms for solid compositions, and preferably from 12 to 18 carbon atoms for liquid compositions. This R² group can be attached to the cationic nitrogen atom through a group containing one, or more, ester, amide, ether, amine, etc., preferably ester, linking groups which can be desirable for increased hydrophilicity, biodegradability, etc. Such linking groups are preferably within about three carbon atoms of the nitrogen atom. Suitable biodegradable single-long-chain alkyl cationic surfactants containing an ester linkage in the long chain are described in U.S. Pat. No. 4,840,738, Hardy and Walley, issued June 20, 1989, said patent being incorporated herein by reference.
If the corresponding, non-quaternary amines are used, any acid (preferably a mineral or polycarboxylic acid) which is added to keep the ester groups stable will also keep the amine protonated in the compositions and preferably during the rinse so that the amine has a cationic group. The composition is buffered (pH from 2 to 5, preferably from 2 to 4) to maintain an appropriate, effective charge density in the aqueous liquid concentrate product and upon further dilution e.g., to form a less concentrated product and/or upon addition to the rinse cycle of a laundry process.
It will be understood that the main function of the water-soluble cationic surfactant is to lower the viscosity and/or increase the dispersibility of the diester softener and it is not, therefore, essential that the cationic surfactant itself have substantial softening properties, although this may be the case. Also, surfactants having only a single long alkyl chain, presumably because they have greater solubility in water, can protect the diester softener from interacting with anionic surfactants and/or detergent builders that are carried over into the rinse.
Other cationic materials with ring structures such as alkyl imidazoline, imidazolinium, pyridine, and pyridinium salts having a single C₁₂-C₃₀ alkyl chain can also be used. Very low pH is required to stabilize, e.g., imidazoline ring structures.
Some alkyl imidazolinium salts useful in the present invention have the general formula:
wherein Y² is -C(O)-O-, -O-(O)-C-, -C(O)-N(R⁵), or -N(R⁵)-C(O)-in which R⁵ is hydrogen or a C₁-C₄ alkyl radical; R⁶ is a C₁-C₄ alkyl radical; R⁷ and R⁸ are each independently selected from R and R² as defined hereinbefore for the single-long-chain cationic surfactant with only one being R².
Some alkyl pyridinium salts useful in the present invention have the general formula:
wherein R² and X^- are as defined above. A typical material of this type is cetyl pyridinium chloride.

(2) Nonionic Surfactant (Alkoxylated Materials)

Suitable nonionic surfactants to serve as the viscosity/dispersibility modifier include addition products of ethylene oxide and, optionally, propylene oxide, with fatty alcohols, fatty acids, fatty amines, etc.
Any of the alkoxylated materials of the particular type described hereinafter can be used as the nonionic surfactant. In general terms, the nonionics herein, when used alone, I. in solid compositions are at a level of from 5% to 20%, preferably from 8% to 15%, and II. in liquid compositions are at a level of from 0% to 5%, preferably from 0.1% to 5%, more preferably from 0.2% to 3%. Suitable compounds are substantially water-soluble surfactants of the general formula: R² - Y - (C₂H₄O)_z - C₂H₄OH wherein R² for both solid and liquid compositions is selected from the group consisting of primary, secondary and branched chain alkyl and/or acyl hydrocarbyl groups; primary, secondary and branched chain alkenyl hydrocarbyl groups; and primary, secondary and branched chain alkyl- and alkenyl-substituted phenolic hydrocarbyl groups; said hydrocarbyl groups having a hydrocarbyl chain length of from 8 to 20, preferably from 10 to 18 carbon atoms. More preferably the hydrocarbyl chain length for liquid compositions is from 16 to 18 carbon atoms and for solid compositions from 10 to 14 carbon atoms. In the general formula for the ethoxylated nonionic surfactants herein, Y is typically -O-, -C(O)O-, -C(O)N(R)-, or -C(O)N(R)R-, In which R², and R, when present, have the meanings given hereinbefore, and/or R can be hydrogen, and z is at least 8, preferably at least 10-11. Performance and, usually, stability of the softener composition decrease when fewer ethoxylate groups are present.
The nonionic surfactants herein are characterized by an HLB (hydrophilic-lipophilic balance) of from 7 to 20, preferably from 8 to 15. Of course, by defining R² and the number of ethoxylate groups, the HLB of the surfactant is, in general, determined. However, it is to be noted that the nonionic ethoxylated surfactants useful herein, for concentrated liquid compositions, contain relatively long chain R² groups and are relatively highly ethoxylated. While shorter alkyl chain surfactants having short ethoxylated groups may possess the requisite HLB, they are not as effective herein.
Nonionic surfactants as the viscosity/dispersibility modifiers are preferred over the other modifiers disclosed herein for compositions with higher levels of perfume.
Examples of nonionic surfactants follow. The nonionic surfactants of this invention are not limited to these examples. In the examples, the integer defines the number of ethoxyl (EO) groups in the molecule.

a. Straight-Chain, Primary Alcohol Alkoxylates

The deca-, undeca-, dodeca-, tetradeca-, and pentadecaethoxylates of n-hexadecanol, and n-octadecanol having an HLB within the range recited herein are useful viscosity/dispersibility modifiers in the context of this invention. Exemplary ethoxylated primary alcohols useful herein as the viscosity/dispersibility modifiers of the compositions are n-C₁₈EO(10); and n-C₁₀EO(11). The ethoxylates of mixed natural or synthetic alcohols in the "tallow" chain length range are also useful herein. Specific examples of such materials include tallowalcohol-EO(11), tallowalcohol-EO(18), and tallowalcohol -EO(25).

b. Straight-Chain, Secondary Alcohol Alkoxylates

The deca-, undeca-, dodeca-, tetradeca-, pentadeca-, octadeca-, and nonadeca-ethoxylates of 3-hexadecanol, 2-octadecanol, 4-eicosanol, and 5-eicosanol having and HLB within the range recited herein are useful viscosity/dispersibility modifiers in the context of this invention. Exemplary ethoxylated secondary alcohols useful herein as the viscosity/dispersibility modifiers of the compositions are: 2-C₁₆EO(11); 2-C₂₀EO(11); and 2-C₁₆EO(14).

c. Alkyl Phenol Alkoxylates

As in the case of the alcohol alkoxylates, the hexa- through octadeca-ethoxylates of alkylated phenols, particularly monohydric alkylphenols, having an HLB within the range recited herein are useful as the viscosity/dispersibility modifiers of the instant compositions. The hexa- through octadeca-ethoxylates of p-tridecylphenol, m-pentadecylphenol, and the like, are useful herein. Exemplary ethoxylated alkylphenols useful as the viscosity/dispersibility modifiers of the mixtures herein are: p-tridecylphenol EO(11) and p-pentadecylphenol EO(18).
As used herein and as generally recognized in the art, a phenylene group in the nonionic formula is the equivalent of an alkylene group containing from 2 to 4 carbon atoms. For present purposes, nonionics containing a phenylene group are considered to contain an equivalent number of carbon atoms calculated as the sum of the carbon atoms in the alkyl group plus about 3.3 carbon atoms for each phenylene group.

d. Olefinic Alkoxylates

The alkenyl alcohols, both primary and secondary, and alkenyl phenols corresponding to those disclosed immediately hereinabove can be ethoxylated to an HLB within the range recited herein and used as the viscosity/dispersibility modifiers of the instant compositions.

e. Branched Chain Alkoxylates

Branched chain primary and secondary alcohols which are available from the well-known "OXO" process can be ethoxylated and employed as the viscosity/dispersibility modifiers of compositions herein.
The above ethoxylated nonionic surfactants are useful in the present compositions alone or in combination, and the term "nonionic surfactant" encompasses mixed nonionic surface active agents.

(3) Amine Oxides

Suitable amine oxides include those with one alkyl or hydroxyalkyl moiety of 8 to 28 carbon atoms, preferably from 8 to 16 carbon atoms, and two alkyl moieties selected from the group consisting of alkyl groups and hydroxyalkyl groups with 1 to 3 carbon atoms.
The amine oxides:
I. in solid compositions are at a level of from 0% to 15%, preferably from 3% to 15%; and
II. in liquid compositions are at a level of from 0% to 5%, preferably from 0.25% to 2%, the total amine oxide present at least at an effective level.
Examples include dimethyloctylamine oxide, diethyldecylamine oxide, bis-(2-hydroxyethyl)dodecylamine oxide, dimethyldodecylamine oxide, dipropyltetradecyl amine oxide, methylethylhexadecylamine oxide, dimethyl-2-hydroxyoctadecylamine oxide, and coconut fatty alkyl dimethylamine oxide.

(4) Fatty Acids

Suitable fatty acids include those containing from 12 to 25, preferably from 13 to 22, more preferably from 16 to 20, total carbon atoms, with the fatty moiety containing from 10 to 22, preferably from 10 to 18, more preferably from 10 to 14 (mid cut), carbon atoms. The shorter moiety contains from 1 to 4, preferably from 1 to 2 carbon atoms.
Fatty acids are present at the levels outlined above for amine oxides. Fatty acids are preferred concentration aids for those compositions which require a concentration aid and contain perfume.

II. Electrolyte Concentration Aids

Inorganic viscosity control agents which can also act like or augment the effect of the surfactant concentration aids, include water-soluble, ionizable salts which can also optionally be incorporated into the compositions of the present invention. A wide variety of ionizable salts can be used. Examples of suitable salts are the halides of the Group IA and IIA metals of the Periodic Table of the Elements, e.g., calcium chloride, magnesium chloride, sodium chloride, potassium bromide, and lithium chloride. The ionizable salts are particularly useful during the process of mixing the ingredients to make the compositions herein, and later to obtain the desired viscosity. The amount of ionizable salts used depends on the amount of active ingredients used in the compositions and can be adjusted according to the desires of the formulator. Typical levels of salts used to control the composition viscosity are from 20 to 20,000 parts per million (ppm), preferably from 20 to 11,000 ppm, by weight of the composition.
Alkylene polyammonium salts can be incorporated into the composition to give viscosity control in addition to or in place of the water-soluble, ionizable salts above. In addition, these agents can act as scavengers, forming ion pairs with anionic detergent carried over from the main wash, in the rinse, and on the fabrics, and may improve softness performance. These agents may stabilize the viscosity over a broader range of temperature, especially at low temperatures, compared to the inorganic electrolytes.
Specific examples of alkylene polyammonium salts include 1-lysine monohydrochloride and 1,5-diammonium 2-methyl pentane dihydrochloride.

(C) Stabilizers

Stabilizers can be present in the compositions of the present invention. The term "stabilizer," as used herein, includes antioxidants and reductive agents. These agents are present at a level of from 0% to 2%, preferably from 0.01% to 0.2%, more preferably from 0.035% to 0.1% for antioxidants, and more preferably from 0.01% to 0.2% for reductive agents. These assure good odor stability under long term storage conditions for the compositions and compounds stored in molten form. Use of antioxidants and reductive agent stabilizers is especially critical for unscented or low scent products (no or low perfume).

Examples of antioxidants that can be added to the compositions of this invention include a mixture of ascorbic acid, ascorbic palmitate, propyl gallate, available from Eastman Chemical Products, Inc., under the trade names Tenox® PG and Tenox S-1; a mixture of BHT (butylated hydroxytoluene), BHA (butylated hydroxyanisole), propyl gallate, and citric acid, available from Eastman Chemical Products, Inc., under the trade name Tenox-6; butylated hydroxytoluene, available from UOP Process Division under the trade name Sustane® BHT; tertiary butylhydroquinone, Eastman Chemical Products, Inc., as Tenox TBHQ; natural tocopherols, Eastman Chemical Products, Inc., as Tenox GT-1/GT-2; and butylated hydroxyanisole, Eastman Chemical Products, Inc., as BHA; long chain esters (C₈-C₂₂) of gallic acid, e.g., dodecyl gallate; Irganox® 1010; Irganox® 1035; Irganox® B 1171; Irganox® 1425; Irganox® 3114; Irganox® 3125; and mixtures thereof; preferably Irganox® 3125, Irganox® 1425, Irganox® 3114, and mixtures thereof; more preferably Irganox® 3125 alone or mixed with citric acid and/or other chelators such as isopropyl citrate, Dequest® 2010, available from Monsanto with a chemical name of 1-hydroxyethylidene-1, 1-diphosphonic acid (etidronic acid), and Tiron®, available from Kodak with a chemical name of 4,5-dihydroxy-m-benzene-sulfonic acid/sodium salt, and DTPA®, available from Aldrich with a chemical name of diethylenetriaminepentaacetic acid.. The chemical names and CAS numbers for some of the above stabilizers are listed in Table II below.

Antioxidant	CAS No.	Chemical Name used in Code of Federal Regulations
Irganox® 1010	6683-19-8	Tetrakis [methylene(3,5-di-tert-butyl-4 hydroxyhydrocinnamate)] methane
Irganox® 1035	41484-35-9	Thiodiethylene bis(3,5-di-tert-butyl-4-hydroxyhydrocinnamate
Irganox® 1098	23128-74-7	N,N'-Hexamethylene bis(3,5-di-tert-butyl-4-hydroxyhydrocinnammamide
Irganox® B 1171	31570-04-4	1:1 Blend of Irganox® 1098 and Irgafos® 168
	23128-74-7
Irganox® 1425	65140-91-2	Calcium bis[monoethyl(3,5-di-tert-butyl-4-hydroxybenzyl) phosphonate]
Irganox® 3114	27676-62-6	1,3,5-Tris(3,5-di-tert-butyl-4-hydroxybenzyl)-s-triazine-2,4,6-(1H, 3H, 5H)trione
Irganox® 3125	34137-09-2	3,5-Di-tert-butyl-4-hydroxyhydrocinnamic acid triester with 1,3,5-tris(2-hydroxyethyl)-S-triazine-2,4,6-(1H, 3H, 5H)-trione
Irgafos® 168	31570-04-4	Tris(2,4-di-tert-butyl-phenyl)phosphite

Examples of reductive agents include sodium borohydride, hypophosphorous acid, Irgafos® 168, and mixtures thereof.

(D) Liquid Carrier

The liquid carrier employed in the instant compositions is preferably at least primarily water due to its low cost relative availability, safety, and environmental compatibility. The level of water in the liquid carrier is at least 50%, preferably at least 60%, by weight of the carrier. The level of liquid carrier is less than 70, preferably less than 65, more preferably less than 50. Mixtures of water and low molecular weight, e.g., <100, organic solvent, e.g., lower alcohol such as ethanol, propanol, isopropanol or butanol are useful as the carrier liquid. Low molecular weight alcohols include monohydric, dihydric (glycol, etc.) trihydric (glycerol, etc.), and higher polyhydric (polyols) alcohols.

(E) Optional Ingredients

(1) Optional Soil Release Agent

Optionally, the compositions herein contain from 0% to 10%, preferably from 0.1% to 5%, more preferably from 0.1% to 2%, of a soil release agent. Preferably, such a soil release agent is a polymer. Polymeric soil release agents useful in the present invention include copolymeric blocks of terephthalate and polyethylene oxide or polypropylene oxide, and the like. U.S. Pat. No. 4,956,447, Gosselink/Hardy/Trinh, issued Sept. 11, 1990, discloses specific preferred soil release agents comprising cationic functionalities, said patent being incorporated herein by reference.
A preferred soil release agent is a copolymer having blocks of terephthalate and polyethylene oxide. More specifically, these polymers are comprised of repeating units of ethylene and/or propylene terephthalate and polyethylene oxide terephthalate at a molar ratio of ethylene terephthalate units to polyethylene oxide terephthalate units of from 25:75 to 35:65, said polyethylene oxide terephthalate containing polyethylene oxide blocks having molecular weights of from 300 to 2000. The molecular weight of this polymeric soil release agent is in the range of from 5,000 to 55,000.
Another preferred polymeric soil release agent is a crystallizable, polyester with repeat units of ethylene terephthalate units containing from 10% to 15% by weight of ethylene terephthalate units together with from 10% to 50% by weight of polyoxyethylene terephthalate units, derived from a polyoxyethylene glycol of average molecular weight of from 300 to 6,000, and the molar ratio of ethylene terephthalate units to polyoxyethylene terephthalate units in the crystallizable polymeric compound is between 2:1 and 6:1. Examples of this polymer include the commercially available materials Zelcon® 4780 (from DuPont) and Milease® T (from ICI).
Highly preferred soil release agents are polymers of the generic formula (I):
in which X can be any suitable capping group, with each X being selected from the group consisting of H, and alkyl or acyl groups containing from about 1 to about 4 carbon atoms, preferably methyl. n is selected for water solubility and generally is from 6 to 113, preferably from 20 to 50. u is critical to formulation in a liquid composition having a relatively high ionic strength. There should be very little material in which u is greater than 10. Furthermore, there should be at least 20%, preferably at least 40%, of material in which u ranges from 3 to 5.
The R¹ moieties are essentially 1,4-phenylene moieties. As used herein, the term "the R¹ moieties are essentially 1,4-phenylene moieties" refers to compounds where the R¹ moieties consist entirely of 1,4-phenylene moieties, or are partially substituted with other arylene or alkarylene moieties, alkylene moieties, alkenylene moieties, or mixtures thereof. Arylene and alkarylene moieties which can be partially substituted for 1,4-phenylene include 1,3-phenylene, 1,2-phenylene, 1,8-naphthylene, 1,4-naphthylene, 2,2-biphenylene, 4,4-biphenylene and mixtures thereof. Alkylene and alkenylene moieties which can be partially substituted include ethylene, 1,2-propylene, 1,4-butylene, 1,5-pentylene, 1,6-hexamethylene, 1,7-heptamethylene, 1,8-octamethylene, 1,4-cyclohexylene, and mixtures thereof.
For the R¹ moieties, the degree of partial substitution with moieties other than 1,4-phenylene should be such that the soil release properties of the compound are not adversely affected to any great extent. Generally, the degree of partial substitution which can be tolerated will depend upon the backbone length of the compound, i.e., longer backbones can have greater partial substitution for 1,4-phenylene moieties. Usually, compounds where the R¹ comprise from 50% to 100% 1,4-phenylene moieties (from 0 to 50% moieties other than 1,4-phenylene) have adequate soil release activity. For example, polyesters made according to the present invention with a 40:60 mole ratio of isophthalic (1,3-phenylene) to terephthalic (1,4-phenylene) acid have adequate soil release activity. However, because most polyesters used in fiber making comprise ethylene terephthalate units, it is usually desirable to minimize the degree of partial substitution with moieties other than 1,4-phenylene for best soil release activity. Preferably, the R¹ moieties consist entirely of (i.e., comprise 100%) 1,4-phenylene moieties, i.e., each R¹ moiety is 1,4-phenylene.
For the R² moieties, suitable ethylene or substituted ethylene moieties include ethylene, 1,2-propylene, 1,2-butylene, 1,2-hexylene, 3-methoxy-1,2-propylene and mixtures thereof. Preferably, the R² moieties are essentially ethylene moieties, 1,2-propylene moieties or mixture thereof. Inclusion of a greater percentage of ethylene moieties tends to improve the soil release activity of compounds. Inclusion of a greater percentage of 1,2-propylene moieties tends to improve the water solubility of the compounds.
Therefore, the use of 1,2-propylene moieties or a similar branched equivalent is desirable for incorporation of any substantial part of the soil release component in the liquid fabric softener compositions. Preferably, from 75% to 100%, more preferably from 90% to 100%, of the R² moieties are 1,2-propylene moieties.
The value for each n is at least 6, and preferably is at least 10. The value for each n usually ranges from 12 to 113. Typically, the value for each n is in the range of from 12 to 43.
A more complete disclosure of these highly preferred soil release agents is contained in European Pat. Application 185,427, Gosselink, published June 25, 1986, incorporated herein by reference.

(2) Optional Bacteriocides

Examples of bacteriocides that can be used in the compositions of this invention are parabens, especially methyl, glutaraldehyde, formaldehyde, 2-bromo-2-nitropropane-1,3-diol sold by Inolex Chemicals under the trade name Bronopol®, and a mixture of 5-chloro-2-methyl-4-isothiazoline-3-one and 2-methyl-4-isothiazoline-3-one sold by Rohm and Haas Company under the trade name Kathon® CG/ICP. Typical levels of bacteriocides used in the present compositions are from about 1 to about 2,000 ppm by weight of the composition, depending on the type of bacteriocide selected. Methyl paraben is especially effective for mold growth in aqueous fabric softening compositions with under 10% by weight of the diester compound.

(3) Other Optional Ingredients

The present invention can include other optional components conventionally used in textile treatment compositions, for example, colorants, perfumes, preservatives, optical brighteners, opacifiers, fabric conditioning agents, surfactants, stabilizers such as guar gum and polyethylene glycol, anti-shrinkage agents, anti-wrinkle agents, fabric crisping agents, spotting agents, germicides, fungicides, anti-corrosion agents, antifoam agents, and the like.
An optional additional softening agent of the present invention is a nonionic fabric softener material. Typically, such nonionic fabric softener materials have an HLB of from 2 to 9, more typically from 3 to 7. Such nonionic fabric softener materials tend to be readily dispersed either by themselves, or when combined with other materials such as single-long-chain alkyl cationic surfactant described in detail hereinbefore. Dispersibility can be improved by using more single-long-chain alkyl cationic surfactant, mixture with other materials as set forth hereinafter, use of hotter water, and/or more agitation. In general, the materials selected should be relatively crystalline, higher melting, (e.g., >-50°C) and relatively water-insoluble.
The level of optional nonionic softener in the solid composition is typically from 10% to 40%, preferably from 15% to 30%, and the ratio of the optional nonionic softener to DEQA is from 1:6 to 1:2, preferably from 1:4 to 1:2. The level of optional nonionic softener in the liquid composition is typically from 0.5% to 10%, preferably from 1% to 5%.
Preferred nonionic softeners are fatty acid partial esters of polyhydric alcohols, or anhydrides thereof,
wherein the alcohol, or anhydride, contains from 2 to 18, preferably from 2 to 8, carbon atoms, and each fatty acid moiety contains from 12 to 30, preferably from 16 to 20, carbon atoms. Typically, such softeners contain from one to 3, preferably 2 fatty acid groups per molecule.
The polyhydric alcohol portion of the ester can be ethylene glycol, glycerol, poly (e.g., di-, tri-, tetra, penta-, and/or hexa-) glycerol, xylitol, sucrose, erythritol, pentaerythritol, sorbitol or sorbitan. Sorbitan esters and polyglycerol monostearate are particularly preferred.
The fatty acid portion of the ester is normally derived from fatty acids having from 12 to 30, preferably from 16 to 20, carbon atoms, typical examples of said fatty acids being lauric acid, myristic acid, palmitic acid, stearic acid and behenic acid.
Highly preferred optional nonionic softening agents for use in the present invention are the sorbitan esters, which are esterified dehydration products of sorbitol, and the glycerol esters.
Sorbitol, which is typically prepared by the catalytic hydrogenation of glucose, can be dehydrated in well known fashion to form mixtures of 1,4- and 1,5-sorbitol anhydrides and small amounts of isosorbides. (See U.S. Pat. No. 2,322,821, Brown, issued June 29, 1943, incorporated herein by reference.)
The foregoing types of complex mixtures of anhydrides of sorbitol are collectively referred to herein as "sorbitan." It will be recognized that this "sorbitan" mixture will also contain some free, uncyclized sorbitol.
The preferred sorbitan softening agents of the type employed herein can be prepared by esterifying the "sorbitan" mixture with a fatty acyl group in standard fashion, e.g., by reaction with a fatty acid halide or fatty acid. The esterification reaction can occur at any of the available hydroxyl groups, and various mono-, di-, etc., esters can be prepared. In fact, mixtures of mono-, di-, tri-, etc., esters almost always result from such reactions, and the stoichiometric ratios of the reactants can be simply adjusted to favor the desired reaction product.
For commercial production of the sorbitan ester materials, etherification and esterification are generally accomplished in the same processing step by reacting sorbitol directly with fatty acids. Such a method of sorbitan ester preparation is described more fully in MacDonald; "Emulsifiers:" Processing and Quality Control:, Journal of the American Oil Chemists' Society, Vol. 45, October 1968.
Details, including formula, of the preferred sorbitan esters can be found in U.S. Pat. No. 4,128,484, incorporated hereinbefore by reference.
Certain derivatives of the preferred sorbitan esters herein, especially the "lower" ethoxylates thereof (i.e., mono-, di-, and tri-esters wherein one or more of the unesterified -OH groups contain one to about twenty oxyethylene moieties [Tweens®] are also useful in the composition of the present invention. Therefore, for purposes of the present invention, the term "sorbitan ester" includes such derivatives.
For the purposes of the present invention, it is preferred that a-significant amount of di- and tri- sorbitan esters are present in the ester mixture. Ester mixtures having from 20-50% mono-ester, 25-50% di-ester and 10-35% of tri- and tetra-esters are preferred.
The material which is sold commercially as sorbitan mono-ester (e.g., monostearate) does in fact contain significant amounts of di- and tri-esters and a typical analysis of sorbitan monostearate indicates that it comprises about 27% mono-, 32% di-and 30% tri- and tetra-esters. Commercial sorbitan monostearate therefore is a preferred material. Mixtures of sorbitan stearate and sorbitan palmitate having stearate/palmitate weight ratios varying between 10:1 and 1:10, and 1,5-sorbitan esters are useful. Both the 1,4- and 1,5-sorbitan esters are useful herein.
Other useful alkyl sorbitan esters for use in the softening compositions herein include sorbitan monolaurate, sorbitan monomyristate, sorbitan monopalmitate, sorbitan monobehenate, sorbitan monooleate, sorbitan dilaurate, sorbitan dimyristate, sorbitan dipalmitate, sorbitan distearate, sorbitan dibehenate, sorbitan dioleate, and mixtures thereof, and mixed tallowalkyl sorbitan mono- and di-esters. Such mixtures are readily prepared by reacting the foregoing hydroxy-substituted sorbitans, particularly the 1,4- and 1,5-sorbitans, with the corresponding acid or acid chloride in a simple esterification reaction. It is to be recognized, of course, that commercial materials prepared in this manner will comprise mixtures usually containing minor proportions of uncyclized sorbitol, fatty acids, polymers, isosorbide structures, and the like. In the present invention, it is preferred that such impurities are present at as low a level as possible.
The preferred sorbitan esters employed herein can contain up to 15% by weight of esters of the C₂₀-C₂₆, and higher, fatty acids, as well as minor amounts of C₈, and lower, fatty esters.
Glycerol and polyglycerol esters, especially glycerol, diglycerol, triglycerol, and polyglycerol mono- and/or di- esters, preferably mono-, are also preferred herein (e.g., polyglycerol monostearate with a trade name of Radiasurf 7248). Glycerol esters can be prepared from naturally occurring triglycerides by normal extraction, purification and/or interesterification processes or by esterification processes of the type set forth hereinbefore for sorbitan esters. Partial esters of glycerin can also be ethoxylated to form usable derivatives that are included within the term "glycerol esters."
Useful glycerol and polyglycerol esters include mono-esters with stearic, oleic, palmitic, lauric, isostearic, myristic, and/or behenic acids and the diesters of stearic, oleic, palmitic, lauric, isostearic, behenic, and/or myristic acids. It is understood that the typical mono-ester contains some di- and tri-ester, etc.
The "glycerol esters" also include the polyglycerol, e.g., diglycerol through octaglycerol esters. The polyglycerol polyols are formed by condensing glycerin or epichlorohydrin together to link the glycerol moieties via ether linkages. The mono- and/or diesters of the polyglycerol polyols are preferred, the fatty acyl groups typically being those described hereinbefore for the sorbitan and glycerol esters.

(F) A Preferred Process for Preparation of Concentrated Aqueous Biodegradable Textile Softener Compositions (Dispersions)

This invention also includes a preferred process for preparing concentrated aqueous biodegradable quaternary ammonium fabric softener compositions/dispersions having ≥28% of biodegradable fabric softener active, including those described in copending U.S. Pat. Application Ser. No. 07/881,979, filed May 12, 1992, Baker et al., said application being incorporated herein by reference. A molten organic premix of the fabric softener active and any other organic materials, but preferably not the perfumes, is dispersed into a water seat at 40°C (104°F). The dispersion is then cooled to -1°C (30°F) to 15.6°C (60F°) above the major thermal transition temperature of the biodegradable fabric softener active. Electrolyte, as described hereinbefore, is then added in a range of from 400 ppm to 7,000 ppm, more preferably from 1,000 ppm to 5,000 ppm, most preferably from 2,000 ppm to 4,000 ppm, at 30F°-60F° above the major thermal transition temperature. High shear milling is conducted at a temperature of from 10°C (50F°) to 15°C (59F°) above the major thermal transition temperature of the biodegradable fabric softener active. The dispersion is then cooled to ambient temperature and the remaining electrolyte is added, typically in an amount of from 600 ppm to 8,000 ppm, more preferably from 2,000 ppm to 5,000 ppm, most preferably from 2,000 ppm to 4,000 ppm at ambient temperature. As a preferred option, perfume is added at ambient temperature before adding the remaining electrolyte.
The said organic premix is, typically, comprised of said biodegradable fabric softener active and, preferably, at least an effective amount of low molecular weight alcohol processing aid, e.g., ethanol or isopropanol, preferably ethanol.
The above described preferred process provides a convenient method for preparing concentrated aqueous biodegradable fabric softener dispersions, as recited herein, when the biodegradable fabric softening composition consists of from 28% to 40%, more preferably from 28% to 35%, most preferably from 28% to 32%, of total biodegradable fabric softener active, and from 1,000 ppm to 15,000 ppm, more preferably from 3,000 ppm to 10,000 ppm, most preferably from 4,000 ppm to 8,000 ppm, of total electrolyte.
In a preferred process for preparing concentrated aqueous biodegradable fabric softener dispersions as described above, the perfume is added at ambient temperature at a concentration of from 0.1% to 2%, preferably from 0.5% to 1.5%, most preferably from 0.8% to 1.4%, by weight of the total aqueous dispersion.
In the method aspect of this invention, fabrics or fibers are contacted with an effective amount, generally from about 10 ml to 150 ml (per 3.5 kg of fiber or fabric being treated) of the softener actives (including diester compound) herein in an aqueous bath. Of course, the amount used is based upon the judgment of the user, depending on concentration of the composition, fiber or fabric-type, degree of softness desired, and the like. Preferably, the rinse bath contains from 10 to 1,000 ppm, preferably from 50 to 500 ppm, of the DEQA fabric softening compounds herein.
The granules can be formed by preparing a melt, solidifying it by cooling, and then grinding and sieving to the desired size. It is highly preferred that the primary particles of the granules have a diameter of from 50 to 1,000, preferably from 50 to 400, more preferably from 50 to 200, microns. The granules can comprise smaller and larger particles, but preferably from 85% to 95%, more preferably from 95% to 100%, are within the indicated ranges. Smaller and larger particles do not provide optimum emulsions/dispersions when added to water. Other methods of preparing the primary particles can be used including spray cooling of the melt. The primary particles can be agglomerated to form a dust-free, non-tacky, free-flowing powder. The agglomeration can take place in a conventional agglomeration unit (i.e., Zig-Zag Blender, Lodige) by means of a water-soluble binder. Examples of water-soluble binders useful in the above agglomeration process include glycerol, polyethylene glycols, polymers such as PVA, polyacrylates, and natural polymers such as sugars.
The flowability of the granules can be improved by treating the surface of the granules with flow improvers such as clay, silica or zeolite particles, water-soluble inorganic salts, starch, etc.

EXAMPLES I and IA

	I	Ia
Component	Wt.%	Wt.%
Diester Compound	26.0	26.0
Hydrochloric Acid	0.018	0.0082
Citric Acid	-	0.005
Liquitint® Blue 651 Dye (1%)	0.25	0.25
Perfume	1.35	1.35
Tenox® S-1	0.10	-
Irganox® 3125	-	0.035
Kathon® (1.5%)	0.02	0.02
DC-2210 Antifoam (10%)	0.15	0.15
CaCl₂ Solution (15%)	4.33	3.33
DI Water	Balance	Balance
pH = 2.8 - 3.5
Viscosity = 35-60 mPa.

The above compositions are made by the following process:
1. Separately, heat the diester compound premix with the Irganox 3125 and the water seat containing HCl, citric acid (if used), and antifoam agent to 73.9 ± 15°C (165 ±5°F); (Note: for la, the citric acid can totally replace HCl, if desired):
2. Add the diester compound premix into the water seat over 5-6 minutes. During the injection, both mix (600-1,000 rpm) and mill (8,000 rpm with an IKA Ultra Turrax T-50 Mill) the batch.
3. Add 500 ppm of CaCl₂ at approximately halfway through the injection.
4. Add 2,000 ppm CaCl₂ over 2-7 minutes (200-2,500 ppm/minute) with mixing at 800-1,000 rpm after premix injection is complete at about 150°-165°F.
5. Add perfume over 30 seconds at 145°-155°F.
6. Add dye and Kathon and mix for 30-60 seconds. Cool batch to 70-80°F.
7. Add 2,500 ppm to 4,000 ppm CaCl₂ to cooled batch and mix.
The fatty acids in Table I, used to make the diester compounds of Examples I and la have the following characteristics. The process of forming the diester compounds is as set forth hereinbefore.
Examples II-VII are diester compounds derived from the fatty acid of Table I, Number 2, with an IV of 53.9 and were stored in molten form. These examples are relative measures of activity and are not absolute values based on HPLC. Examples II, IV, and VI initially contain 15.9% ethanol and 0.21% water. Examples III, V, and VII initially contain 18.8% isopropyl alcohol and 0.2% water.

EXAMPLE II

	(120°F/49°C)
	Fresh	1 Wk	3 Wks
	Wt.%	Wt.%	Wt.%
Diester	69	64	67
Monoester	9	8	9

EXAMPLE III

	(120°F/49°C)
	Fresh	1 Wk	3 Wks
	Wt.%	Wt.%	Wt.%
Diester	68	71	67
Monoester	9	9	9

EXAMPLE IV

	(150°F/66°C)
	Fresh	1 Wk	3 Wks
	Wt.%	Wt.%	Wt.%
Diester	69	68	67
Monoester	9	8	9

EXAMPLE V

	(150°F/66°C)
	Fresh	1 Wk	3 Wks
	Wt.%	Wt.%	Wt.%
Diester	68	67	68
Monoester	9	9	10

EXAMPLE VI

	(180°F/82°C)
	Fresh	1 Wk	3 Wks
	Wt.%	Wt.%	Wt.%
Diester	69	67	61
Monoester	9	11	15

EXAMPLE VII

	(180°F/82°C)
	Fresh	1 Wk	3 Wks
	Wt.%	Wt.%	Wt.%
Diester	68	65	61
Monoester	9	11	13

No degradation is observed over 3 weeks storage at 120°F/49°C to 150°F/66°C. About 10% relative degradation is observed over 3 weeks at 180°F/82°C.

EXAMPLE VIII

	Wt.%	Wt.%	Wt.%	Wt.%
Diester Compound	32	32	32	32
Hydrochloric Acid	-	-	-	0.10
DC-2210 Antifoam (10%)	0.10	0.10	0.10	0.10
CaCl₂ Solution (15%)	5.0	5.0	5.0	5.0
Coco Choline Ester	1.00	-	-	-
Tallow Choline Ester	-	1.00	-	-
Coco Fatty Acid	-	-	0.25	-
Coco Dimethyl Amine Oxide	-	-	-	1.00
DI Water	61.65	61.65	62.40	61.55

The above compositions are made by the following process:
(A) inject the diester compound premix plus fatty acid, having a temperature of from 54.5°C (130°F) to 87.8°C (190°F), preferably 60-71.1°C (140-160°F), into an acid water seat, plus choline ester or amine oxide (when present) and antifoam (when present), having a temperature of from 54.5°C (130°F) to 87.8°C (190°F); preferably 60-71.1°C (140-160°F), under agitation over about 3 minutes.
(B) add about 3,750 ppm of CaCl₂ over 5 minutes solution after premix injection is complete and temperature has dropped to 37.8-54.4°C (100-130°F);
(C) mill composition for 2 minutes at 7,000 rpm (IKA Ultra Turrax Mill) after CaCl₂ addition;
(D) add about 3,750 ppm of CaCl₂ solution after the batch is cooled to a temperature of from 55°F to 95°F.
If inclusion of perfume in the composition is desired, the perfume is preferably added either during or after milling step (C), and after the temperature drops to ≤(130°F) 54.4°C.

EXAMPLE IX

Solid Particulate Compositions Plus Water to Form Liquid Compositions

	1	2	3
Component	Wt.%	Wt.%	Wt.%
Diester Compound	8.1	7.74	6.00
Ethoxylated Fatty Alcohol	0.5	0.86	-
PGMS	-	-	1.74
Coconut Choline Ester Chloride	-	-	0.86
Minors (Perfume; Antifoam)	0.35	0.35	0.35

EXAMPLE IX - Continued

	4	5	6
Component	Wt.%	Wt.%	Wt.%
Diester Compound	7.6	7.6	7.6
Ethoxylated Fatty Alcohol	1	1	1

EXAMPLE IX - Continued

	7	8	9
Component	Wt.%	Wt.%	Wt.%
Diester Compound	7.6	8.1	23.5
Ethoxylated Fatty Alcohol	1	-	-
PGMS
Coconut Choline Ester Chloride	-	0.5	2.5
Minors (Perfume; Antifoam)	-	0.35	1.5
Electrolyte	-	-	0.4

The above liquid compositions are made from the corresponding solid compositions having the same active material, on a 100% active weight basis, by the procedure given below. This shows the surprising ability of the solid particulate compositions herein to effectively disperse following simple addition to lukewarm water with gentle agitation (e.g., manual shaking). Improved results are obtained by using higher temperatures and/or effective mixing conditions, e.g., high shear mixing, milling, etc. However, even the mild conditions provide acceptable aqueous compositions.

Procedure

Molten diester is mixed with molten ethoxylated fatty alcohol or molten coconut choline ester chloride. In No. 3, molten PGMS is also added. The mixture is cooled and solidified by pouring onto a metal plate, and then ground. The solvent is removed by a Rotovapor® (2 hrs. at 40-50°C at maximum vacuum). The resulting powder is ground and sieved. The reconstitution of the powder is standardized as follows:
The total active solid is 8.6% (diester plus ethoxylated fatty alcohol). Tap water is heated to 35°C (95°F). Antifoam is added to the water. The active powder is mixed with the perfume powder. This mix is sprinkled on the water under continuous agitation (up to 2,000 rpm for 10 minutes). This product is cooled by means of a cooling spiral prior to storage. The fresh product is transferred to a bottle and left standing to cool.

EXAMPLE X

Viscosity Stability of Compositions Containing Diester Compound

	A	B
Component	Wt.%	Wt.%
Diester Compound	20	20
CaCl₂	0.072	0.072
HCl	0.07	0.07
DI Water	Balance	Balance

Viscosity (m Pas)
		4°C	10°C	Ambient	35°C
A	Fresh	-	-	30	-
	3 days	680	28	25	30
	1 week	Gel	800	20	32
	2 weeks	Gel	Gel	15	48
B	Fresh	-	-	27	-
	3 days	35	32	25	32
	1 week	40	34	25	27
	2 weeks	52	35	27	30

EXAMPLE XI

Concentrated Diester Compositions with Low Temperature Stability

Component	Wt.%
Diester Compound	22.7
PGMS	3.5
Tallow alcohol ethoxylate (25)	1.5
Soil Release Polymer	0.33
Silicone Antifoam	0.019
CaCl₂	0.29
HCl	0.08
PEG 4000	0.60
Minors	1.00
DI Water	Balance

EXAMPLE XII

Stable Molten Diester Compounds

	A	B	C	D
Component	Wt%	Wt.%	Wt.%	Wt.%
Diester Compound	77.0	76.0	76.5	77.0
Monoester Compound	4.0	6.1	7.0	7.0
Diesteramine and Diesteramine HCl	3.2	3.0	2.4	2.5
Fatty Acid	1.5	0.5	0.5	0.3
Isopropyl Alcohol	14.0	14.0	-	-
Ethanol	-	-	13.1	13.6
Water	0.1	0.2	0.4	0.1
BHT	0.1	0.1	-	-
Propyl Gallate	-	-	0.1	-
Irganox® 3125	-	-	-	0.05
Citric Acid	0.10	0.10	0.05	0.005
Totals	100.0	100.0	100.0	100.0
IV of Fatty Acid	18	55	47	56

EXAMPLE XIII

Example XIII is diester compound derived from fatty acid of Table I, No. 1, with an IV of 43 stored in molten form. These are relative measures of active based on HPLC. The initial ethanol level is approximately 12-13% in each sample. The sample containing 0.2% by weight water shows better storage stability at 3 weeks.

	(150°F/66°C)
	Fresh	3 Wks
	Wt.%	Wt.%
Diester	76	75
Monoester	8	9
Water	0.2	0.53
Diester	77	74
Monoester	9	10
Water	0.68	0.71
Diester	76	73
Monoester	9	12
Water	1.1	1.23
Diester	76	71
Monoester	9	12
Water	1.7	1.42

EXAMPLE XIV

	Wt.%	Wt.%	Wt.%	Wt.%
Diester Compound	32	32	32	32
Hydrochloric Acid	0.04	0.04	0.04	0.01
DC-2210 Antifoam (10%)	0.10	0.10	0.10	0.10
CaCl₂	0.75	0.75	0.75	0.80
Coco Fatty Acid	1.5	0.25	0.25	-
Ethanol	3.90	4.50	4.90	5.25
Perfume	1.35	1.35	1.35	1.35
DI water	60.40	61.10	60.70	60.50

The above compositions are made by the following process:
1. Injecting the premix* into an acid water seat and milling at 70-75°C; adding 500 ppm of CaCl₂ at 70°C; adding 3,500 ppm of CaCl₂ at 65°C;adding perfume at 63°C;and adding 3,500 ppm of CaCl₂ at 25°C.
2. Injecting the premix into an acid water seat and milling at 70-75°C; adding 500 ppm of CaCl₂ at 70°C; adding 3,500 ppm of CaCl₂ at 60°C; adding 3,500 ppm of CaCl₂ at 24°C; and adding perfume at 23°C.
3. Injecting the premix into an acid water seat at 70-75°C; adding 500 ppm of CaCl₂ at 70°C; adding 2,500 ppm of CaCl₂ at 40°C; adding 4,500 ppm of CaCl₂ at 23°C; milling at 22°C; and adding perfume at 22°C.
4. Injecting the premix into an acid water seat at 60°C; adding 3,750 ppm of CaCl₂ at 40°C; milling at 30°C; adding 3,750 ppm of CaCl₂ at 23°C; and adding perfume at 23°C.
5. Injecting the premix into an acid water seat at 60°C; adding 3,750 ppm of CaCl₂ at 40°C; adding perfume and milling at 30°C; and adding 3,750 ppm of CaCl₂ at 23°C.
6. Injecting the premix into an acid water seat at 60°C; adding 3,750 ppm of CaCl₂ at 40°C; milling at 32°C; adding perfume at 23°C; and adding 3,750 ppm of CaCl₂ at 23°C.
7. Injecting the premix** into an acid water seat at 65°C; adding 4,000 ppm of CaCl₂ at 40°C; milling at 33°C; adding perfume at 23°C; and adding 4,000 ppm of CaCl at 23°C.

EXAMPLE XIV - Continued

Composition	Process Key	Initial Viscosity	Aged Viscosity	Dispersed Phase Volume
I	1	Cream	--	NA
II	2	448 cp	--	NA
II	3	143 cp	390 mPa (5 days)	NA
III	4	58 cp	333 mPa (3 days)	73-74%
III	5	145 cp	175 mPa (13 days)	71%
III	6	125 cp	162 mPa (13 days)	66-67%
IV	7	112 cp	125 mPa (14 days)	68%

Claims

A quaternary ammonium compound having the structure: (R)_4-m - N⁺ -[(CH₂)_n - Y - R²]_m X^- wherein
each Y is -O-(O)C-, or -C(O)-O-;
m is 2;
n is 1 to 4;
each R is a C₁-C₆ alkyl group, benzyl group, or mixtures thereof;
each R² is a C₁₁-C₂₁ hydrocarbyl or substituted hydrocarbyl substituent, derived from fatty acid having at least 90% C₁₆-C₁₈ chainlength; and
X- is any softener-compatible anion;
wherein the compound is derived from C₁₂-C₂₂ fatty acyl groups having an Iodine Value of from greater than 20 to less than 100, preferably from 20 to 65, more preferably from 40 to 60, for optimum static control; the level of unsaturation of the fatty acyl groups is less than 65% by weight, wherein said compounds are capable of forming concentrated aqueous compositions with concentrations greater than 13% by weight without viscosity modifiers other than normal polar organic solvents present in the raw material of the compound or added electrolyte; wherein any fatty acyl groups from tallow must be modified by partial hydrogenation; wherein the cis/trans isomer weight ratio is greater than 80/20.
A quaternary ammonium compound having the structure: (R)_4-m - N⁺ -[(CH₂)_n - Y - R²]_m X^- wherein
each Y is -O-(O)C-, or -C(O)-O-;
m is 2;
n is 1 to 4;
each R is a C₁-C₆ alkyl group, benzyl group, or mixtures thereof;
each R² is a C₁₁-C₂₁ hydrocarbyl or substituted hydrocarbyl substituent, derived from fatty acid having at least 90% C₁₆-C₁₈ chainlength; and
X^- is any softener-compatible anion;
wherein the compound is derived from C₁₂-C₂₂ fatty acyl groups having an Iodine Value of from greater than 5 to less than 25, preferably from 10 to 25, more preferably from 15 to 20, for optimum low temperature stability; and the cis/trans isomer weight ratio is 70/30 or greater.
A stable, homogeneous fabric softening composition selected from the group consisting of:

I. a solid particulate composition comprising:

(A) from 50% to 95%, preferably from 60% to 90%, of biodegradable quaternary ammonium fabric softening compound; and

(B) from 0% to 30% of a dispersibility modifier selected from the group consisting of:

1. C₁₀-C₂₂ single-long-chain-alkyl, cationic surfactant, preferably coco choline ester, tallow choline ester, and mixtures thereof;

2. nonionic surfactant with at least 8 ethoxy moieties, preferably C₁₀-C₁₄ alcohol, with poly(10-18)ethoxylate;

3. amine oxide, preferably cocoamine oxide;

4. C₁₂-C₂₅ fatty acid, preferably coco fatty acid; and

5. mixtures thereof; and

(C) from 0% to 2% of a stabilizer, preferably selected from the group consisting of ascorbic acid, propyl galate, ascorbic palmitate, butylated hydroxytoluene, tertiary butylhydoquinone, natural tocopherols, butylated hydroxyanisole, citric acid, C₈-C₂₂ esters of gallic acid, Irganox® 1010, Irganox® 1035, Irganox® B 1171, Irganox® 1425, Irganox® 3114, Irganox® 3125, and mixtures thereof; and

II. a liquid composition comprising:

(A) from 5% to 50% of biodegradable quaternary ammonium fabric softening compound;

(B) from 0% to 5% of a dispersibility modifier selected from the group consisting of:

1. C₁₀-C₂₂ single-long-chain-alkyl, cationic surfactant, preferably coco choline ester or tallow choline ester, and mixtures thereof;

2. nonionic surfactant with at least 8 ethoxy moieties, preferably C₁₀-C₁₄ alcohol, with poly(10-18)ethoxylate;

3. amine oxide, preferably cocoamine oxide;

4. C₁₂-C₂₅ fatty acid, preferably coco fatty acid; and

5. mixtures thereof; and

(C) from 0% to 2% of a stabilizer, preferably selected from the group consisting of ascorbic acid, propyl galate, ascorbic palmitate, butylated hydroxytoluene, tertiary butylhydoquinone, natural tocopherols, butylated hydroxyanisole, citric acid, C₈-C₂₂ esters of gallic acid, Irganox® 1010, Irganox® 1035, Irganox® B 1171, Irganox® 1425, Irganox® 3114, Irganox® 3125, and mixtures thereof; and

(D) aqueous liquid carrier;

wherein the quaternary ammonium fabric softening compound has the formula: (R)_4-m - N⁺ -[(CH₂)_n - Y - R²]_m X^- 0 wherein
each Y is -O-(O)C-, or -C(O)-O-;
m is 2;
n is 1 to 4;
each R is a C₁-C₆ alkyl group, benzyl group, or mixtures thereof;
each R² is a C₁₁-C₂₁ hydrocarbyl or substituted hydrocarbyl substituent, derived from fatty acid having at least 90% C₁₆-C₁₈ chainlength; and
X^- is any softener-compatible anion;
wherein the compound is derived from C₁₂-C₂₂ fatty acyl groups having an Iodine Value of from greater than 5 to less than 25, preferably from 10 to 25, more preferably from 15 to 20, for optimum low temperature stability; the level of unsaturation of the fatty acyl groups is less than 65% by weight; the cis /trans isomer weight ratio is 70/30 or greater; wherein the pH of the liquid composition is from 2 to 5; wherein preferably for I., the particle size is from 50 to 1,000 microns; wherein the dispersibility modifier affects the composition's viscosity, dispersibility, or both; and preferably wherein the composition comprises an effective amount, up to 10%, of soil release polymer.
The compounds and composition according to any one of the preceding claim wherein the polyunsaturation content of the fatty acyl groups is less than 5% by weight, preferably less than 1% by weight.
A process of making the liquid softening composition of Claim 3 or a liquid composition comprising:

(A) from 5% to 50%, preferably from 15% to 50%, of biodegradable quaternary ammonium fabric softening compound;

(B) from 0% to 5% of a dispersibility modifier selected from the group consisting of:

1. C₁₀-C₂₂ single-long-chain-alkyl, cationic surfactant, preferably coco choline ester or tallow choline ester;

2. nonionic surfactant with at least 8 ethoxy moieties, preferably C₁₀-C₁₄ alcohol, with poly(10-18)ethoxylate;

3. amine oxide, preferably cocoamine oxide;

4. C₁₂-C₂₅ fatty acid, preferably coco fatty acid; and

5. mixtures thereof; and

(C) from 0% to 2% of a stabilizer, preferably selected from the group consisting of ascorbic acid, propyl galate, ascorbic palmitate, butylated hydroxytoluene, tertiary butylhydoquinone, natural tocopherols, butylated hydroxyanisole, citric acid, C₈-C₂₂ esters of gallic acid, Irganox® 1010, Irganox® 1035, Irganox® B 1171, Irganox® 1425, Irganox® 3114, Irganox® 3125, and mixtures thereof; and

(D) an aqueous liquid carrier;

wherein the quaternary ammonium fabric softening compound has the formula: (R)_4-m - N⁺ -[(CH₂)_n - Y - R²]_m X^- wherein
each Y is -O-(O)C-, or -C(O)-O-;
m is 2;
n is 1 to 4;
each R is a C₁-C₆ alkyl group, benzyl group, or mixtures thereof;
each R² is a C₁₁-C₂₁ hydrocarbyl or substituted hydrocarbyl substituent, derived from .fatty acid having at least 90% C₁₆-C₁₈ chainlength; and
X^- is any softener-compatible anion;
wherein the compound is derived from C₁₂-C₂₂ fatty acyl groups having an Iodine Value of from greater than 20 to less than 100, preferably from 20 to 65, more preferably from 40 to 60, for optimum static control; the level of unsaturation of the fatty acyl groups is less than 65% by weight; the liquid compositions being stable without nonionic viscosity modifiers when the concentration is less than or equal to 13%; wherein preferably the composition additionally comprises an effective amount, up to 10%, of a soil release polymer; and wherein the dispersibility modifier affects the composition's viscosity, dispersibility, or both;
wherein said process comprises the steps of:

(A) injecting the quaternary ammonium fabric softening compound premix, having a temperature of from 130°F to 190°F, preferably from 155°F to 175°F, into an acid water seat, having a temperature of from 130°F to 190°F, preferably 155°F to 175°F;

(B) mixing and milling the batch during the injection;

(C) adding from 0 ppm to 1,000 ppm, preferably 500 to 600 ppm, of CaCl₂ at from 1/2 to 2/3 of the way through the injection time;

(D) adding from 1,000 ppm to 5,000 ppm, preferably 2,000 to 4,000 ppm, of CaCl₂ after premix injection is complete, preferably wherein the injection rate is from 200 to 2,500 ppm per minute over a total of from 2 to 7 minutes;

(E) adding perfume at a temperature of from 105°F to 160°F, preferably 145°F to 155°F; and

(F) adding from 1,000 ppm to 5,000 ppm, preferably 2,000 to 4,000 ppm, CaCl₂ after the batch is cooled to a temperature of from 55°F to 95°F, preferably 65°F to 85°F;

wherein the total CaCl₂ in the composition is from 2,000 ppm to 11,000 ppm, preferably 6,000 ppm to 7,500 ppm; and wherein the composition does not contain a viscosity modifier.
A process of making the liquid softening composition of Claim 3 or a liquid composition comprising:

(A) from 5% to 50%, preferably from 15% to 50%, of biodegradable quaternary ammonium fabric softening compound;

(B) from 0% to 5% of a dispersibility modifier selected from the group consisting of:

1. C₁₀-C₂₂ single-long-chain-alkyl, cationic surfactant, preferably coco choline ester or tallow choline ester;

2. nonionic surfactant with at least 8 ethoxy moieties, preferably C₁₀-C₁₄ alcohol, with poly(10-18)ethoxylate;

3. amine oxide, preferably cocoamine oxide;

4. C₁₂-C₂₅ fatty acid, preferably coco fatty acid; and

5. mixtures thereof; and

(C) from 0% to 2% of a stabilizer, preferably selected from the group consisting of ascorbic acid, propyl galate, ascorbic palmitate, butylated hydroxytoluene, tertiary butylhydoquinone, natural tocopherols, butylated hydroxyanisole, citric acid, C₈-C₂₂ esters of gallic acid, Irganox®. 1010, Irganox® 1035, Irganox® B 1171, Irganox® 1425, Irganox® 3114, Irganox® 3125, and mixtures thereof; and

(D) an aqueous liquid carrier;

wherein the quaternary ammonium fabric softening compound has the formula: (R)_4-m - N⁺-[(CH₂)_n - Y - R²]_m X^- wherein
each Y is -O-(O)C-, or -C(O)-O-;
m is 2;
n is 1 to 4;
each R is a C₁-C₆ alkyl group, benzyl group, or mixtures thereof;
each R² is a C₁₁-C₂₁ hydrocarbyl or substituted hydrocarbyl substituent, preferably derived from fatty acid having at least 90% C₁₆-C₁₈ chainlength; and
X^- is any softener-compatible anion;
wherein the compound is derived from C₁₂-C₂₂ fatty acyl groups having an Iodine Value of from greater than 20 to less than 100, preferably from 20 to 65, more preferably from 40 to 60, for optimum static control; the level of unsaturation of the fatty acyl groups is less than 65% by weight; the liquid composition being stable wihout nonionic viscosity modifiers when the concentration is less than or equal to 13%; wherein preferably the composition additionally comprises an effective amount, up to 10%, of a soil release polymer; and wherein the dispersibility modifier affects the compositions viscosity, dispersibility, or both;
wherein said process comprises the steps of:

(A) injecting the quaternary ammonium fabric softening compound premix, having a temperature of from 130°F to 190°F, into an acid water seat, having a temperature of from 130°F to 190°F;

(B) adding from 1,000 ppm to 5,000 ppm of CaCl₂ at a temperature of from 100°F to 130°F;

(C) milling the composition; and

(D) adding from 1,000 ppm to 5,000 ppm CaCl₂ after the batch is cooled to a temperature of from 55°F to 95°F;

wherein the total CaCl₂ in the composition is from 2,000 ppm to 11,000 ppm; and wherein the perfume is added either during or after Step (C) but before Step (D) and after the temperature has dropped to ≤ 130°F.
A color and odor stable, molten fabric softening raw material comprising:

(A) from 0,1% to 92% biodegradable quaternary ammonium fabric softener compound as defined in Claim 5;

(B) from 8% to 18%, preferably from 12% to 16%, alcohol solvent;

(C) from 0% to 2% of a stabilizer, preferably 0.01% to 0.2% of a reductive agent stabilizer, from 0.035% to 0.1% of an antioxidant stabilizer, and mixtures thereof;

wherein the water level is less than 1%, preferably less than 0.5%;
wherein preferably the alcohol is selected from the group consisting of ethanol, isopropyl alcohol, propylene glycol, ethylene glycol, and mixtures thereof; and wherein the stabilizer is preferably selected from the group consisting of ascorbic acid, propyl galate, ascorbic palmitate, butylated hydroxytoluene, tertiary butylhydoquinone, natural tocopherols, butylated hydroxyanisole, sodium borohydride, hypophosphorous acid, isopropyl citrate, C₈-C₂₂ esters of gallic acid, Irganox® 1010, Irganox® 1035, Irganox® B 1171, Irganox® 1425, Irganox® 3114, Irganox® 3125, Irgafos® 168, and mixtures thereof.
A process for preparing a concentrated aqueous biodegradable quaternary ammonium fabric softening composition in the form of dispersions having ≥ 28% of biodegradable quaternary ammonium fabric softener active which comprises:

(A) dispensing an organic premix into the water seat at about 150°F; wherein said organic premix is comprised of:

(1) a biodegradable quaternary ammonium fabric softener; and

(2) an effective amount of low molecular weight alcohol processing aid;

(B) cooling the resulting dispersion to a temperature from about 30°F to about 60°F above the major thermal transition temperature of the biodegradable quaternary ammonium fabric softener;

(C) adding from about 400 ppm to about 7,000 ppm of electrolyte at a temperature of from about 30°F to about 60°F above the thermal transition temperature of the biodegradable fabric softener and preferably high shear milling; and

(D) cooling the dispersion to ambient temperature and then adding additional electrolyte, in an amount of from about 600 ppm to about 8,000 ppm;

wherein the quaternary ammonium fabric softener is as defined in Claim 5;
wherein preferably perfume is added during Step (D) after cooling to ambient and before adding the remaining electrolyte; wherein preferably the composition is substantially free of viscosity and dispersibility modifiers other than low molecular weight alcohols, electrolytes, and perfume; and
wherein preferably the total level of electrolyte is from 1,000 ppm to 15,000 ppm.